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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Abdominal- und Thoraxbandage — 223 UDI-DI variants, MDR

MD Atlas
Werkmeister GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Abdominal- und Thoraxbandage

4048486051101Y8

223 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Werkmeister GmbH + Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4048486051101Y8
Device name: Abdominal- und Thoraxbandage
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: Werkmeister GmbH + Co. KG
SRN: DE-MF-000005120
Country: Germany
Email: info@werkmeister-gmbh.de
Phone: +49 (0) 5655 98 99 0

Variants by status

UDI-DI variants

223 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K2F944YMYQGJKMQET1ZQXHZF

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

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316204048486126841
326504048486126780
316504048486117863
316104048486117788
326204048486117962
326404048486126766
326104048486126711
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9034604048486165062
112304048486195496
112504048486195519
112204048486195489
112404048486195502
112104048486195472

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